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Presence Current · Arkansas
Last published 2026
Sources OpenAlex · ORCID
Refreshed 2026-08-16

Pritmohinder S. Gill

High Impact

Associate Professor

Faculty Researcher

21 h-index 47 pubs 2,197 cited

  • Humans
  • Animals
  • Male
  • RNA, Messenger
  • Acetaminophen
  • Chemical and Drug Induced Liver Injury
  • Child
  • Female
  • Rats
  • MicroRNAs
  • Hypertension, Renal
  • NADPH Oxidases
  • Blood Pressure
  • Mice, Inbred C57BL
  • Mice

Biography and Research Information

OverviewAI-generated summary

Pritmohinder S. Gill's research investigates the molecular underpinnings of neurodevelopmental disorders, with a particular focus on autism spectrum disorder (ASD). His work utilizes integrated transcriptomic profiling, examining both mRNA and microRNA expression, to identify novel targets and networks associated with these conditions. Recent publications explore the role of microRNAs in immunomodulation within ASD and the transcriptomic signatures of mitochondrial dysfunction in affected individuals.

His research also extends to the practical implementation of pharmacogenomics in clinical settings. Gill has contributed to studies assessing the integration of pharmacogenomics into multidisciplinary teams, including experiences at Arkansas Children’s Hospital. His scholarship metrics include an h-index of 21, with over 2,193 total citations across 47 publications, designating him as a highly cited researcher. Key collaborators include Shannon Rose and Jeffery L. Clothier from the University of Arkansas for Medical Sciences.

Metrics

  • h-index: 21
  • Publications: 47
  • Citations: 2,197

Selected Publications

  • Transcriptomic Signatures of Mitochondrial Dysfunction in Autism: Integrated mRNA and microRNA Profiling (2025)
    Genes 1 citation DOI OpenAlex
  • Pharmacogenetics (2024)
    Elsevier eBooks DOI OpenAlex
  • Contributors (2024)
    Elsevier eBooks DOI OpenAlex
  • Integrated microRNA–mRNA Expression Profiling Identifies Novel Targets and Networks Associated with Autism (2022)
    Journal of Personalized Medicine 14 citations DOI OpenAlex
  • Identification of DCAF1 by Clinical Exome Sequencing and Methylation Analysis as a Candidate Gene for Autism and Intellectual Disability: A Case Report (2022)
    Journal of Personalized Medicine 2 citations DOI OpenAlex
  • Multidisciplinary Consulting Team for Complicated Cases of Neurodevelopmental and Neurobehavioral Disorders: Assessing the Opportunities and Challenges of Integrating Pharmacogenomics into a Team Setting (2022)
    Journal of Personalized Medicine 7 citations DOI OpenAlex
  • MicroRNA Expression Profiles in Autism Spectrum Disorder: Role for miR-181 in Immunomodulation (2021)
    Journal of Personalized Medicine 21 citations DOI OpenAlex
  • Molecular Dysregulation in Autism Spectrum Disorder (2021)
    Journal of Personalized Medicine 22 citations DOI OpenAlex
  • Implementing Pharmacogenomics Testing: Single Center Experience at Arkansas Children’s Hospital (2021)
    Journal of Personalized Medicine 25 citations DOI OpenAlex
  • Acetaminophen is both bronchodilatory and bronchoprotective in human precision cut lung slice airways (2018)
    Xenobiotica 7 citations DOI OpenAlex
  • Acylcarnitines as Translational Biomarkers of Mitochondrial Dysfunction (2018)
    6 citations DOI OpenAlex
  • Multiple microRNAs function as self-protective modules in acetaminophen-induced hepatotoxicity in humans (2017)
    Archives of Toxicology 64 citations DOI OpenAlex
  • Autistic Siblings with Novel Mutations in Two Different Genes: Insight for Genetic Workups of Autistic Siblings and Connection to Mitochondrial Dysfunction (2017)
    Frontiers in Pediatrics 36 citations DOI OpenAlex
  • MicroRNA regulation of CYP 1A2, CYP3A4 and CYP2E1 expression in acetaminophen toxicity (2017)
    Scientific Reports 64 citations DOI OpenAlex
  • Metabolomics Analysis of Urine Samples from Children after Acetaminophen Overdose (2017)
    Metabolites 18 citations DOI OpenAlex

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Collaboration Network

56 Collaborators 29 Institutions 10 Countries

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